Canonical Allele Identifier: CA1176721883
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750545A= , CM000663.2:g.75750545A= GRCh38
NC_000001.10:g.76216230A= , CM000663.1:g.76216230A= GRCh37
NC_000001.9:g.75988818A= NCBI36
NG_007045.2:g.31188A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.944A= MANE Select ENSP00000359878.5:p.Glu315=
ENST00000473018.3:n.3068A=
ENST00000532207.6:n.1833A=
ENST00000541113.6:c.849+986A= ENSP00000442324.2:n.849+986A=
ENST00000679509.1:n.1906A=
ENST00000679530.1:c.*712A= ENSP00000506454.1:n.*712A=
ENST00000679615.1:n.2959A=
ENST00000679687.1:c.506A= ENSP00000506598.1:p.Glu169=
ENST00000679704.1:c.*710A= ENSP00000505117.1:n.*710A=
ENST00000679709.1:c.*907A= ENSP00000506623.1:n.*907A=
ENST00000679976.1:c.*528A= ENSP00000505565.1:n.*528A=
ENST00000680166.1:n.4233A=
ENST00000680315.1:n.827A=
ENST00000680517.1:c.*332A= ENSP00000505803.1:n.*332A=
ENST00000680582.1:n.1906A=
ENST00000680613.1:c.*315A= ENSP00000506114.1:n.*315A=
ENST00000680662.1:c.*858A= ENSP00000505080.1:n.*858A=
ENST00000680691.1:c.*607A= ENSP00000506487.1:n.*607A=
ENST00000680694.1:c.*532A= ENSP00000505658.1:n.*532A=
ENST00000680743.1:c.*611A= ENSP00000505073.1:n.*611A=
ENST00000680749.1:c.*229A= ENSP00000505122.1:n.*229A=
ENST00000680798.1:c.*419A= ENSP00000505670.1:n.*419A=
ENST00000680805.1:c.803A= ENSP00000505447.1:p.Glu268=
ENST00000680844.1:c.*728A= ENSP00000506541.1:n.*728A=
ENST00000680948.1:c.*811A= ENSP00000505441.1:n.*811A=
ENST00000680964.1:c.944A= ENSP00000505961.1:p.Glu315=
ENST00000681037.1:c.*2428A= ENSP00000506025.1:n.*2428A=
ENST00000681063.1:c.*91A= ENSP00000506616.1:n.*91A=
ENST00000681209.1:c.*599A= ENSP00000505877.1:n.*599A=
ENST00000681278.1:n.1301A=
ENST00000681289.1:n.4939A=
ENST00000681361.1:c.*611A= ENSP00000506679.1:n.*611A=
ENST00000681430.1:c.944A= ENSP00000506301.1:p.Glu315=
ENST00000681446.1:c.*526A= ENSP00000506244.1:n.*526A=
ENST00000681450.1:c.*615A= ENSP00000505660.1:n.*615A=
ENST00000681548.1:c.*530A= ENSP00000505275.1:n.*530A=
ENST00000681616.1:c.*603A= ENSP00000505111.1:n.*603A=
ENST00000681621.1:c.*528A= ENSP00000505770.1:n.*528A=
ENST00000681680.1:n.3039A=
ENST00000681720.1:c.*399A= ENSP00000505438.1:n.*399A=
ENST00000681730.1:n.1166A=
ENST00000681790.1:c.686A= ENSP00000505130.1:p.Glu229=
ENST00000681837.1:n.1560A=
ENST00000681913.1:n.3068A=
ENST00000681916.1:c.*712A= ENSP00000506477.1:n.*712A=
ENST00000681930.1:n.3068A=
ENST00000370834.9:c.1043A= ENSP00000359871.5:p.Glu348=
ENST00000370841.8:c.944A= ENSP00000359878.4:p.Glu315=
ENST00000420607.6:c.956A= ENSP00000409612.2:p.Glu319=
ENST00000481374.1:n.95A=
ENST00000525808.5:c.*530A= ENSP00000434823.1:n.*530A=
ENST00000526129.5:c.*728A= ENSP00000434092.1:n.*728A=
ENST00000526196.5:c.*712A= ENSP00000431953.1:n.*712A=
ENST00000528016.1:c.158A= ENSP00000434284.1:p.Glu53=
ENST00000529059.5:n.853A=
ENST00000532207.5:n.674A=
ENST00000534334.5:c.*528A= ENSP00000435584.1:n.*528A=
ENST00000541113.5:c.836A= ENSP00000442324.1:p.Glu279=
NM_000016.5:c.944A= NP_000007.1:p.Glu315=
NM_001127328.2:c.956A= NP_001120800.1:p.Glu319=
NM_001286042.1:c.836A= NP_001272971.1:p.Glu279=
NM_001286043.1:c.1043A= NP_001272972.1:p.Glu348=
NM_001286044.1:c.377A= NP_001272973.1:p.Glu126=
NM_000016.6:c.944A= MANE Select NP_000007.1:p.Glu315=
NM_001127328.3:c.956A= NP_001120800.1:p.Glu319=
NM_001286042.2:c.836A= NP_001272971.1:p.Glu279=
NM_001286043.2:c.1043A= NP_001272972.1:p.Glu348=
NM_001286044.2:c.377A= NP_001272973.1:p.Glu126=